- Expiry Date: 17 December 2021
Work schedule is Monday – Friday General Shift
The centralized TMF organization is responsible for the completeness and accuracy of the Trial Master File.
Minimum of Bachelor’s degree in a scientific or related discipline
At least 5 years of TMF experience required, including experience in study start-up, maintenance and closeout, and performing quality and completeness reviews.
Relevant experience in clinical trials related roles (i.e. clinical operations and project management).
Extensive knowledge and application of ALCOA+ standards, Good Clinical Practice, Good Documentation Practices and International Council for Harmonization guidelines (E6(R2))
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ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.